4.8 Article

Gestational diabetes mellitus is associated with the neonatal gut microbiota and metabolome

Journal

BMC MEDICINE
Volume 19, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s12916-021-01991-w

Keywords

Gestational diabetes mellitus; Microbiota; Metabolome

Funding

  1. National Natural Science Foundation [81872650]
  2. fifth phase of 333 High-level Talent Training Project of the Jiangsu Province
  3. Nanjing Medical Science and Technique Development Foundation [QRX17162]
  4. Nanjing Science and technology development project [201911040]
  5. Nanjing medical science and technology development fund [ZKX19044]
  6. Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD)

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This study revealed significant changes in the meconium microbiota of neonates born to mothers with gestational diabetes mellitus (GDM), with a reduction in alpha diversity and alterations in the abundance of Firmicutes and Proteobacteria. Metabolomic analysis showed changes in metabolic pathways such as taurine and hypotaurine metabolism, pyrimidine metabolism, beta-alanine metabolism, and bile acid biosynthesis in GDM subjects. The findings highlight the impact of maternal factors on early-life metabolism.
Background Gestational diabetes mellitus (GDM) is a metabolic disease that occurs in pregnant women and increases the risk for the development of diabetes. The relationship between GDM and meconium microbiota and metabolome remains incompletely understood. Methods Four hundred eighteen mothers (147 women with GDM and 271 normal pregnant women) and their neonates from the GDM Mother and Child Study were included in this study. Meconium microbiota were profiled by 16S rRNA gene sequencing. Meconium and maternal serum metabolome were examined by UPLC-QE. Results Microbial communities in meconium were significantly altered in neonates from the GDM mothers. A reduction in alpha diversity was observed in neonates of GDM mothers. At the phylum level, the abundance of Firmicutes and Proteobacteria changed significantly in neonates of GDM mothers. Metabolomic analysis of meconium showed that metabolic pathways including taurine and hypotaurine metabolism, pyrimidine metabolism, beta-alanine metabolism, and bile acid biosynthesis were altered in GDM subjects. Several changed metabolites varying by the similar trend across the maternal serum and neonatal meconium were observed. Conclusion Altogether, these findings suggest that GDM could alter the serum metabolome and is associated with the neonatal meconium microbiota and metabolome, highlighting the importance of maternal factors on early-life metabolism.

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